Valeryl chloride → HCID 54240508, compound
Reaction equation
[C:1]1([CH:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:8]([NH2:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:17]([C:21](Cl)=[O:22])[CH2:18][CH2:19][CH3:20]>>[C:1]1([CH:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:8]([NH:10][C:21](=[O:22])[CH2:17][CH2:18][CH2:19][CH3:20])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
The title compound, white solid, m.p. 83° C. and MS: m/e=296.3 (M+H+) was prepared in accordance with the general method of example 39 from 2,2-diphenylacetamide and butanecarboxylic acid chloride.
Sources & evidence
- ORD record
- ord-eeae5903f0134fb2b4b87fe619e49885
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06803381B1
Reaction notes
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